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Novel Pullulan/Gellan Gum Bilayer Film as a Vehicle for Silibinin-Loaded Nanocapsules in the Topical Treatment of Atopic Dermatitis

In this study a novel gellan gum/pullulan bilayer film containing silibinin-loaded nanocapsules was developed for topical treatment of atopic dermatitis (AD). The bilayer films were produced by applying a pullulan layer on a gellan gum layer incorporated with silibinin nanocapsules by two-step solve...

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Autores principales: Gehrcke, Mailine, Martins, Carolina Cristóvão, de Bastos Brum, Taíne, da Rosa, Lucas Saldanha, Luchese, Cristiane, Wilhelm, Ethel Antunes, Soares, Fabio Zovico Maxnuck, Cruz, Letícia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699506/
https://www.ncbi.nlm.nih.gov/pubmed/36365170
http://dx.doi.org/10.3390/pharmaceutics14112352
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author Gehrcke, Mailine
Martins, Carolina Cristóvão
de Bastos Brum, Taíne
da Rosa, Lucas Saldanha
Luchese, Cristiane
Wilhelm, Ethel Antunes
Soares, Fabio Zovico Maxnuck
Cruz, Letícia
author_facet Gehrcke, Mailine
Martins, Carolina Cristóvão
de Bastos Brum, Taíne
da Rosa, Lucas Saldanha
Luchese, Cristiane
Wilhelm, Ethel Antunes
Soares, Fabio Zovico Maxnuck
Cruz, Letícia
author_sort Gehrcke, Mailine
collection PubMed
description In this study a novel gellan gum/pullulan bilayer film containing silibinin-loaded nanocapsules was developed for topical treatment of atopic dermatitis (AD). The bilayer films were produced by applying a pullulan layer on a gellan gum layer incorporated with silibinin nanocapsules by two-step solvent casting method. The bilayer formation was confirmed by microscopic analysis. In vitro studies showed that pullulan imparts bioadhesitvity for the films and the presence of nanocapsules increased their occlusion factor almost 2-fold. Besides, the nano-based film presented a slow silibinin release and high affinity for cutaneous tissue. Moreover, this film presented high scavenger capacity and non-hemolytic property. In the in vivo study, interestingly, the treatments with vehicle film attenuated the scratching behavior and the ear edema in mice induced by 2,4-dinitrochlorobenzene (DNCB). However, the nano-based film containing silibinin modulated the inflammatory and oxidative parameters in a similar or more pronounced way than silibinin solution and vehicle film, as well as than hydrocortisone, a classical treatment of AD. In conclusion, these data suggest that itself gellan gum/pullulan bilayer film might attenuate the effects induced by DNCB, acting together with silibinin-loaded nanocapsules, which protected the skin from oxidative damage, improving the therapeutic effect in this AD-model.
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spelling pubmed-96995062022-11-26 Novel Pullulan/Gellan Gum Bilayer Film as a Vehicle for Silibinin-Loaded Nanocapsules in the Topical Treatment of Atopic Dermatitis Gehrcke, Mailine Martins, Carolina Cristóvão de Bastos Brum, Taíne da Rosa, Lucas Saldanha Luchese, Cristiane Wilhelm, Ethel Antunes Soares, Fabio Zovico Maxnuck Cruz, Letícia Pharmaceutics Article In this study a novel gellan gum/pullulan bilayer film containing silibinin-loaded nanocapsules was developed for topical treatment of atopic dermatitis (AD). The bilayer films were produced by applying a pullulan layer on a gellan gum layer incorporated with silibinin nanocapsules by two-step solvent casting method. The bilayer formation was confirmed by microscopic analysis. In vitro studies showed that pullulan imparts bioadhesitvity for the films and the presence of nanocapsules increased their occlusion factor almost 2-fold. Besides, the nano-based film presented a slow silibinin release and high affinity for cutaneous tissue. Moreover, this film presented high scavenger capacity and non-hemolytic property. In the in vivo study, interestingly, the treatments with vehicle film attenuated the scratching behavior and the ear edema in mice induced by 2,4-dinitrochlorobenzene (DNCB). However, the nano-based film containing silibinin modulated the inflammatory and oxidative parameters in a similar or more pronounced way than silibinin solution and vehicle film, as well as than hydrocortisone, a classical treatment of AD. In conclusion, these data suggest that itself gellan gum/pullulan bilayer film might attenuate the effects induced by DNCB, acting together with silibinin-loaded nanocapsules, which protected the skin from oxidative damage, improving the therapeutic effect in this AD-model. MDPI 2022-10-31 /pmc/articles/PMC9699506/ /pubmed/36365170 http://dx.doi.org/10.3390/pharmaceutics14112352 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gehrcke, Mailine
Martins, Carolina Cristóvão
de Bastos Brum, Taíne
da Rosa, Lucas Saldanha
Luchese, Cristiane
Wilhelm, Ethel Antunes
Soares, Fabio Zovico Maxnuck
Cruz, Letícia
Novel Pullulan/Gellan Gum Bilayer Film as a Vehicle for Silibinin-Loaded Nanocapsules in the Topical Treatment of Atopic Dermatitis
title Novel Pullulan/Gellan Gum Bilayer Film as a Vehicle for Silibinin-Loaded Nanocapsules in the Topical Treatment of Atopic Dermatitis
title_full Novel Pullulan/Gellan Gum Bilayer Film as a Vehicle for Silibinin-Loaded Nanocapsules in the Topical Treatment of Atopic Dermatitis
title_fullStr Novel Pullulan/Gellan Gum Bilayer Film as a Vehicle for Silibinin-Loaded Nanocapsules in the Topical Treatment of Atopic Dermatitis
title_full_unstemmed Novel Pullulan/Gellan Gum Bilayer Film as a Vehicle for Silibinin-Loaded Nanocapsules in the Topical Treatment of Atopic Dermatitis
title_short Novel Pullulan/Gellan Gum Bilayer Film as a Vehicle for Silibinin-Loaded Nanocapsules in the Topical Treatment of Atopic Dermatitis
title_sort novel pullulan/gellan gum bilayer film as a vehicle for silibinin-loaded nanocapsules in the topical treatment of atopic dermatitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699506/
https://www.ncbi.nlm.nih.gov/pubmed/36365170
http://dx.doi.org/10.3390/pharmaceutics14112352
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